SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Inborn error of metabolism  86095007

Disorder of peroxisomal function  238059005

Loss of multiple peroxisomal functions   238063003

SNOMED CT code


SNOMED code238063003
nameLoss of multiple peroxisomal functions
statusactive
date introduced2002-01-31
fully specified name(s)Loss of multiple peroxisomal functions (disorder)
synonymsLoss of multiple peroxisomal functions
attributes - group1
OccurrenceCongenital   255399007
parentsDisorder of peroxisomal function   238059005
children
  • Pseudoinfantile Refsum's disease   238065005
  • Rhizomelic chondrodysplasia punctata syndrome   56692003
  • Zellweger's-like syndrome   238064009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Disorder of peroxisomal function   238059005
            Loss of multiple peroxisomal functions   238063003

ancestors
sorted most to least specific
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